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  4. NDC Product Code: 62756-218 Ibandronate Sodium

NDC 62756-218 Ibandronate Sodium

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62756-218?
  4. Ibandronate Sodium Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62756-218
Proprietary Name:
Ibandronate Sodium
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sun Pharmaceutical Industries, Inc.
Labeler Code:
62756
Product Label ID:
be514be6-727a-4d6c-993b-52144f8e6de8
Start Marketing Date: [9]
02-15-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62756-218-40

Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON / 3 mL in 1 VIAL, SINGLE-DOSE

Product Details

What is NDC 62756-218?

The NDC code 62756-218 is assigned by the FDA to the product Ibandronate Sodium which is product labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62756-218-40 1 vial, single-dose in 1 carton / 3 ml in 1 vial, single-dose. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Ibandronate Sodium?

Ibandronate is used to prevent and treat certain types of bone loss (osteoporosis). Osteoporosis causes bones to become thinner and break more easily. Your chance of developing osteoporosis increases after menopause, as you age, or if you take corticosteroid medications (such as prednisone) for long periods. This medication works by slowing bone loss to help maintain strong bones and reduce the risk of broken bones (fractures). Ibandronate belongs to a class of medications called bisphosphonates.

Which are Ibandronate Sodium UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Ibandronate Sodium Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Ibandronate Sodium?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 904955 - ibandronate sodium 3 MG in 3 ML Injection
  • RxCUI: 904955 - 3 ML ibandronic acid 1 MG/ML Injection
  • RxCUI: 904955 - ibandronic acid 1 MG/ML (as ibandronate sodium 1.13 MG/ML) Injection
  • RxCUI: 904955 - ibandronic acid 3 MG per 3 ML (as ibandronate sodium 1.13 MG/ML) Injection

* Please review the disclaimer below.

Patient Education

Ibandronate Injection


Ibandronate injection is used to treat osteoporosis (a condition in which the bones become thin and weak and break easily) in women who have undergone menopause (''change of life;'' end of menstrual periods). Ibandronate is in a class of medications called bisphosphonates. It works by preventing bone breakdown and increasing bone density (thickness).
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* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".